Meunier I - Search Results

1

Generation of a human iPSC line, INMi004-A, with a point mutation in CRX associated with autosomal dominant Leber congenital amaurosis.

Erkilic N, Sanjurjo-Soriano C, Manes G, Dubois G, Hamel CP, Meunier I, Kalatzis V. Erkilic N, et al. Among authors: meunier i. Stem Cell Res. 2019 Jul;38:101476. doi: 10.1016/j.scr.2019.101476. Epub 2019 Jun 3. Stem Cell Res. 2019. PMID: 31247521 Free article.

2

[Congenital dystrophy: unilateral involvement in vitelliform retinal dystrophy or Best disease].

Meunier I, Ben Salah S, Arndt C, Hamel C. Meunier I, et al. J Fr Ophtalmol. 2008 Jun;31(6 Pt 1):640-1. doi: 10.1016/s0181-5512(08)75471-8. J Fr Ophtalmol. 2008. PMID: 18772821 French. No abstract available.

3

[Retinitis pigmentosa and central serous choroiditis. Retinal imaging and optical coherence tomography views].

Meunier I, Ben Salah S, Arndt C, Hamel C. Meunier I, et al. J Fr Ophtalmol. 2008 Sep;31(7):735. doi: 10.1016/s0181-5512(08)74392-4. J Fr Ophtalmol. 2008. PMID: 18971860 French. No abstract available.

4

Extensive macular atrophy with pseudodrusen-like appearance: a new clinical entity.

Hamel CP, Meunier I, Arndt C, Ben Salah S, Lopez S, Bazalgette C, Bazalgette C, Zanlonghi X, Arnaud B, Defoort-Dellhemmes S, Puech B. Hamel CP, et al. Among authors: meunier i. Am J Ophthalmol. 2009 Apr;147(4):609-20. doi: 10.1016/j.ajo.2008.10.022. Epub 2009 Feb 1. Am J Ophthalmol. 2009. PMID: 19181301

5

Electrophysiological retinal pigment epithelium changes observed with indocyanine green, trypan blue and triamcinolone.

Arndt C, Meunier I, Rebollo O, Martinenq C, Hamel C, Hattenbach LO. Arndt C, et al. Among authors: meunier i. Ophthalmic Res. 2010;44(1):17-23. doi: 10.1159/000279437. Epub 2010 Feb 3. Ophthalmic Res. 2010. PMID: 20130442

6

Screening genes of the visual cycle RGR, RBP1 and RBP3 identifies rare sequence variations.

Ksantini M, Sénéchal A, Bocquet B, Meunier I, Brabet P, Hamel CP. Ksantini M, et al. Among authors: meunier i. Ophthalmic Genet. 2010 Dec;31(4):200-4. doi: 10.3109/13816810.2010.512354. Ophthalmic Genet. 2010. PMID: 21067480

7

Systematic screening of BEST1 and PRPH2 in juvenile and adult vitelliform macular dystrophies: a rationale for molecular analysis.

Meunier I, Sénéchal A, Dhaenens CM, Arndt C, Puech B, Defoort-Dhellemmes S, Manes G, Chazalette D, Mazoir E, Bocquet B, Hamel CP. Meunier I, et al. Ophthalmology. 2011 Jun;118(6):1130-6. doi: 10.1016/j.ophtha.2010.10.010. Epub 2011 Jan 26. Ophthalmology. 2011. PMID: 21269699

8

A novel locus (CORD12) for autosomal dominant cone-rod dystrophy on chromosome 2q24.2-2q33.1.

Manes G, Hebrard M, Bocquet B, Meunier I, Coustes-Chazalette D, Sénéchal A, Bolland-Augé A, Zelenika D, Hamel CP. Manes G, et al. Among authors: meunier i. BMC Med Genet. 2011 Apr 15;12:54. doi: 10.1186/1471-2350-12-54. BMC Med Genet. 2011. PMID: 21496248 Free PMC article.

9

Cataract as a phenotypic marker for a mutation in WFS1, the Wolfram syndrome gene.

Titah SM, Meunier I, Blanchet C, Lopez S, Rondouin G, Lenaers G, Amati-Bonneau P, Reynier P, Paquis-Flucklinger V, Hamel CP. Titah SM, et al. Among authors: meunier i. Eur J Ophthalmol. 2012 Mar-Apr;22(2):254-8. doi: 10.5301/EJO.2011.8370. Eur J Ophthalmol. 2012. PMID: 21623591 Free article.

10

Combining gene mapping and phenotype assessment for fast mutation finding in non-consanguineous autosomal recessive retinitis pigmentosa families.

Hebrard M, Manes G, Bocquet B, Meunier I, Coustes-Chazalette D, Hérald E, Sénéchal A, Bolland-Augé A, Zelenika D, Hamel CP. Hebrard M, et al. Among authors: meunier i. Eur J Hum Genet. 2011 Dec;19(12):1256-63. doi: 10.1038/ejhg.2011.133. Epub 2011 Jul 27. Eur J Hum Genet. 2011. PMID: 21792230 Free PMC article.

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